Chronisense Medical, Ltd. - FDA 510(k) Cleared Devices

Chronisense Medical, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Yokneam Illit, IL.

Last cleared in 2022. Active since 2022. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Chronisense Medical, Ltd. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by RQM+ as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.